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Volumn 132, Issue 41, 2010, Pages 14603-14616

Controlled orientation of polyconjugated guest molecules in tunable host cavities

Author keywords

[No Author keywords available]

Indexed keywords

AB INITIO; ABSORPTION AND EMISSION SPECTRA; BATHOCHROMIC SHIFT; BI-LAYER STRUCTURE; BILAYER ARCHITECTURE; BITHIOPHENES; BUILDING BLOCKES; CONFORMATIONAL CONSTRAINTS; CONTROLLED ORIENTATION; D-CHANNEL; FRAMEWORK ARCHITECTURE; GUANIDINIUM; GUEST MOLECULES; GUEST-HOST INTERACTIONS; HIGH ASPECT RATIO; HOST-GUESTS; INCLUSION COMPOUNDS; LONG AXIS; METHANOL SOLUTION; MOLECULAR PARAMETERS; PACKING MOTIFS; SULFUR ATOMS; TEMPLATING;

EID: 77958030553     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja106106d     Document Type: Article
Times cited : (60)

References (128)
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    • The various architectural isomers can be distinguished by their "projection topologies", which describe the "up/down" arrangement of the pillars projecting from the sulfonate nodes on the GS sheets. For a detailed discussion, see ref 20
    • The various architectural isomers can be distinguished by their "projection topologies", which describe the "up/down" arrangement of the pillars projecting from the sulfonate nodes on the GS sheets. For a detailed discussion, see ref 20.
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    • These architectures include simple bilayer, crisscross bilayer, simple brick, zigzag brick, double brick, V-brick, double zigzag brick, chevron brick, and the chevron bilayer
    • These architectures include simple bilayer, crisscross bilayer, simple brick, zigzag brick, double brick, V-brick, double zigzag brick, chevron brick, and the chevron bilayer.
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    • g) of the guest, accounting for the van der Waals radii
    • g) of the guest, accounting for the van der Waals radii.
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    • B T at room temperature). These relatively small barriers suggest that multiple conformers coexist in solution and in the gas phase (Figure S8, Supporting Information). Also see
    • B T at room temperature). These relatively small barriers suggest that multiple conformers coexist in solution and in the gas phase (Figure S8, Supporting Information). Also see
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    • The minimum energy conformation for free trans -stilbene and trans -azobenzene is reported as planar, as found in the GDS inclusion compounds. Consequently, the contribution of conformational effects to the bathochromic shifts for these compounds is negligible
    • The minimum energy conformation for free trans -stilbene and trans -azobenzene is reported as planar, as found in the GDS inclusion compounds. Consequently, the contribution of conformational effects to the bathochromic shifts for these compounds is negligible.
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    • A small red shift (<2 nm) has been reported for bithiophene with increasing solvent polarity. See
    • A small red shift (<2 nm) has been reported for bithiophene with increasing solvent polarity. See
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    • 2 BBDS inclusion compound. These results further reinforce a more important role for host-guest interactions in the bathochromic shifts compared with guest-guest interactions
    • 2 BBDS inclusion compound. These results further reinforce a more important role for host-guest interactions in the bathochromic shifts compared with guest-guest interactions.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.